Slucare Department Of Internal Medicine | |
1225 South Grand 2l, Door 3,4 St Louis MO 63104 | |
(314) 977-6164 | |
Not Available |
Full Name | Slucare Department Of Internal Medicine |
---|---|
Speciality | Internal Medicine |
Location | 1225 South Grand, St Louis, Missouri |
Authorized Official Name and Position | Alyce Lanxon (EXECUTIVE DIRECTOR) |
Authorized Official Contact | 3149776828 |
Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
Mailing Address | Practice Location Address |
---|---|
Slucare Department Of Internal Medicine 3545 Lindell Blvd Fl 3 Saint Louis MO 63103-1020 Ph: (314) 977-6828 | Slucare Department Of Internal Medicine 1225 South Grand 2l, Door 3,4 St Louis MO 63104 Ph: (314) 977-6164 |
NPI Number | 1013980366 |
---|---|
Provider Enumeration Date | 02/08/2006 |
Last Update Date | 09/21/2021 |
Identifier | Type | State | Issuer |
---|---|---|---|
1013980366 | NPI | - | NPPES |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
207R00000X | Internal Medicine | (* (Not Available)) | Primary |
2085N0904X | Radiology - Nuclear Radiology | (* (Not Available)) | Secondary |
News Archive
PuriCore, the water-based clean technology company focused on developing and commercializing proprietary, green solutions that safely, effectively, and naturally kill infectious pathogens, today announced its Final Results for the year ending December 31, 2009, and the availability of its 2009 annual report on its website.
The first large epidemiological study to assess the age-old belief that alcohol consumption increases the risk of gout is published in the April 2004 issue of THE LANCET. A prospective study of nearly 50,000 men showed that beer drinking was more likely to be associated with gout than spirits; whereas moderate wine consumption was not linked to a risk of the disease.
A new report shows that only 2-percent (291) of the nation's 13,513 substance abuse treatment facilities provide counseling services in various Asian languages. The report also showed that the proportion of facilities offering these services varied by geographic region.
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Tarsa Therapeutics, Inc. today announced progress in the ORACAL trial of its oral calcitonin product for the treatment of postmenopausal osteoporosis. The company has completed patient enrollment in this multinational, randomized, double-blind, placebo-controlled Phase III trial designed to enroll approximately 550 patients. In addition, Tarsa announced that the independent Data Monitoring Committee (DMC) for the ORACAL trial has completed two separate safety reviews of patient data and recommended that the trial proceed as planned.
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